CA2061835C - Histone promoters - Google Patents
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- CA2061835C CA2061835C CA002061835A CA2061835A CA2061835C CA 2061835 C CA2061835 C CA 2061835C CA 002061835 A CA002061835 A CA 002061835A CA 2061835 A CA2061835 A CA 2061835A CA 2061835 C CA2061835 C CA 2061835C
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- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
- C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
- C12N15/8216—Methods for controlling, regulating or enhancing expression of transgenes in plant cells
- C12N15/8222—Developmentally regulated expression systems, tissue, organ specific, temporal or spatial regulation
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- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
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- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/415—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from plants
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- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
- C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
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- C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
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Abstract
1) Gène chimère pour conférer aux plantes une tolérance accrue vis â vis d'un herbicide. 2) Il comprend, dans le sens de la transcription, une zone promotrice, une zone peptide de transit, une séquence codant pour la tolérance au glyphosate et une zone signal de polyadénylation, caractérisé en ce que la zone promotrice est constituée d'au moins un promoteur d'un gène végétal d'histone permettant l'expression de la protéine de tolérance herbicide dans les zones d'accumulation du glyphosate. 3)production de plantes tolérantes au glyphosate.1) Chimeric gene to give plants increased tolerance to a herbicide. 2) It comprises, in the direction of transcription, a promoter zone, a transit peptide zone, a coding sequence for glyphosate tolerance and a polyadenylation signal zone, characterized in that the promoter zone consists of at least a promoter of a histone plant gene for the expression of the herbicidal tolerance protein in the glyphosate accumulation zones. 3) production of glyphosate tolerant plants.
Description
PROMOTEURS U'HISTQbïE
La présente invention concerne de nouveaux promoteurs,de nouveaux gènes chimères les contenant et leur utilisation dans les plantes pour leur conférer une tolérance accrue à des herbicides .Elle concerne également les cellules végétales transformées à l'aide de ces gènes et les plantes transformées régénérées à partir de ces cellules ainsi que les plantes issues de croisements utilisant ces plantes transformées.
Le glyphosate le sulfosate ou la fosamétine sont des herbicides systémiques à large spectre de la famille des phosphonométhylglycines.Ils agissent essentiellement comme inhibiteurs compétitifs de la 5-enol pyruvylshikimate-3-phosphate synthase (EC U'HISTQBIE PROMOTERS
The present invention relates to new promoters, new chimeric genes the container and their use in plants for give them increased tolerance to herbicides .It also relates to plant cells transformed using these genes and plants regenerated transforms from these cells as well that plants derived from crosses using these transformed plants.
Glyphosate sulfosate or fosametine are broad-spectrum systemic herbicides of the family of phosphonomethylglycines.They act essentially as competitive inhibitors of the 5-enol pyruvylshikimate-3-phosphate synthase (EC
2.5.1.19) ou EPSPS vis à vis du PEP
(phosphoenolpyruvate). Après leur application sur la plante,ils sont véhiculés dans la plante où ils s'accumulent dans les parties à croissance rapide, notamment les apex caulinaires et racinaires,provoquant l'altération jusqu'à la destruction des plantes sensibles.
L'EPSPS plastidiale, cible principale de ces produits est une enzyme de la voie de biosynthèse des acides aminés aromatiques,qui est codée par un ou des gènes nucléaires et synthétisée sous forme d'un précurseur cytoplasmique puis importée dans les plastes où elle s'accumule sous sa forme mature.
La tolérance des plantes au glyphosate et aux produits de la famille est obtenue par introduction stable dans leur génome d'un gène d'EPSPS d'origine végétale ou bactérienne mutée ou non quant aux caractéristiques d'inhibition par le glyphosate du produit de ce gène.Etant donné le mode d'action du glyphosate, il est intéressant de pouvoir exprimer le produit de la traduction de ce gène de façon à
permettre son accumulation importante dans les plastes.
Il est connu,par exemple d'après le brevet américain 4 535 060,de conférer à une plante une tolérance à un herbicide du type ci-dessus,en particulier la N-phosphonométhylglycine ou glyphosate,par introduction dans le génome des plantes d'un gène codant pour une EPSPS portant au moins une mutation rendant cette enzyme plus résistante à son inhibiteur compétitif(le glyphosate), après localisation de l'enzyme dans le compartiment plastidial.Ces techniques demandent cependant à être améliorées pour obtenir une plus grande fiabilité dans l'emploi de ces plantes en conditions agronomiques.
Dans la présente description,on entend par "plante" tout organisme multicellulaire différencié
capable de photosynthèse et par "cellule végétale"
toute cellule issue d'une plante et pouvant constituer des tissus indifférenciés tels que des cals ou des tissus différenciés tels que des embryons ou des parties de plantes des plantes ou des semences.
La présente invention a pour objet la production de plantes transformées ayant une tolérance accrue aux herbicides en général et particulièrement à
ceux de la famille des phosphonométhylglycines par régénération de cellules transformées à l'aide de nouveaux gènes chimères comportant un gène de tolérance à ces herbicides.L'invention concerne également ces nouveaux gènes chimères ainsi que des plantes transformées plus tolérantes en raison d'une meilleure tolérance des parties à croissance rapide ainsi que les 2.5.1.19) or EPSPS with respect to PEP
(Phosphoenolpyruvate). After their application on the plant, they are conveyed in the plant where they accumulate in fast growing parts, especially the stem and root apices, causing alteration to destruction of plants sensitive.
Plastidial EPSPS, the main target of these products is an enzyme of the pathway of biosynthesis of aromatic amino acids, which is coded by one or more nuclear genes and synthesized as a cytoplasmic precursor and then imported into plastids where it accumulates in its mature form.
The tolerance of plants to glyphosate and family products is obtained by introduction stable in their genome an original EPSPS gene plant or bacterial mutated or otherwise as to inhibition characteristics by the glyphosate of the product of this gene.Because of the mode of action of glyphosate, it is interesting to be able to express the product of the translation of this gene so as to allow its significant accumulation in plastids.
It is known, for example according to the patent 4 535 060 to confer on a plant a tolerance to a herbicide of the above type, particularly N-phosphonomethylglycine or glyphosate, by introduction into the genome of plants of a gene coding for an EPSPS carrying at least one mutation making this enzyme more resistant to its competitive inhibitor (glyphosate), after localization of the enzyme in the compartment However, these techniques need to be improved to achieve greater reliability in the use of these plants under agronomic conditions.
In the present description, the term "plant" any differentiated multicellular organism capable of photosynthesis and by "plant cell"
any cell from a plant that may constitute undifferentiated tissues such as calli or differentiated tissues such as embryos or plant parts of plants or seeds.
The present invention relates to the production of transformed plants with tolerance increased use of herbicides in general and particularly those of the phosphonomethylglycine family by regeneration of transformed cells using new chimeric genes with a tolerance gene These inventions also relate to these new chimeric genes as well as plants transformed more tolerant because of better tolerance of fast-growing parties as well as
3 plantes issues de croisements utilisant ces plantes transformées. Elle a également pour objet de nouveaux promoteurs pour la construction des gènes chimères ci-dessus.
Plus particulièrement l'invention a pour objet un gène chimère pour conférer aux plantes une tolérance accrue vis à vis d'un herbicide ayant pour cible l'EPSPS, comprenant, dans le sens de la transcription, une zone promotrice, une zone peptide de transit, une sequence codant pour une enzyme de tolérance au glyphosate et une zone signal de polyadénylation, caractérisé en ce que la zone promotrice est constituée d'au moins un fragment d'un promoteur d'un gène d'histone végétal permettant l'expression préférentielle de la protéine de tolérance herbicide dans les zones d'accumulation du glyphosate.
Dans une forme préférée, l'invention comprends une cellule végétale transformée, comprenant un gène chimère comprenant, dans le sens de la transcription, une zone promotrice, une zone peptide de transit, une séquence codant une protéine de tolérance vis-à-vis d'un herbicide s'accumulant dans les tissus à croissance rapide des plantes, et une zone signal de polyadénylation, caractérisé en ce que la zone promotrice comprend au moins un promoteur d'un gène d'histone végétal permettant l'expression de la protéine de tolérance vis-à-vis d'un herbicide dans les zones d'accumulation dudit herbicide dans les plantes, ladite tolérance herbicide des plantes transformées obtenues à
partir desdites cellules végétales transformées étant améliorée par rapport à des plantes ne comprenant pas ledit gène chimère.
Dans une autre forme préférée, l'invention comprends une procédé pour améliorer la tolérance des plantes aux herbicides, comprenant (i) transformer des 3a cellules végétales avec un gène chimère comprenant, dans le sens de la transcription, une zone promotrice, une zone peptide de transit, une séquence codant une protéine de tolérance vis-à-vis d'un herbicide s'accumulant dans les tissus à croissance rapide des plantes, et une zone signal de polyadénylation, caractérisé en ce que la zone promotrice comprend au moins un promoteur d'un gène d'histone végétal permettant l'expression de la protéine de tolérance vis-à-vis d'un herbicide dans les zones d'accumulation dudit herbicide dans les plantes.
Dans une autre forme préférée, l'invention comprends l'utilisation d'un gène chimère comprenant, dans le sens de la transcription, une zone promotrice, une zone peptide de transit, une séquence codant une protéine de tolérance vis-à-vis d'un herbicide s'accumulant dans les tissus à croissance rapide des plantes, et une zone signal de polyadénylation, pour améliorer la tolérance des plantes vis-à-vis des herbicides, caractérisé en ce que la zone promotrice comprend au moins un promoteur d'un gène d'histone végétal permettant l'expression de la protéine de tolérance vis-à-vis d'un herbicide dans les zones d'accumulation dudit herbicide dans les plantes.
Le gène d'histone provient d'une plante monodicotylédone telle que par exemple le blé, le maïs ou le riz ou de préférence d'une plante dicotylédone telle que par exemple la luzerne, le tournesol, le soja, le colza ou de préférence Arabidopsis thaliana. Cf Plant Mol.. Biol. Vol 8, 1987 p 179-191 Chaboute et al.
On utilise de préférence un gène d'histone du type H3 ou de préférence H4, seuls ou sous une forme multiple, en particulier double.
La zone promotrice du gène chimère selon l'invention peut comprendre en outre avantageusement au 3b moins un fragment d'un promoteur d'un gène s'exprimant naturellement dans les plantes c'est à dire, par exemple une promoteur d'origine virale tel que le promoteur de l'ARN 35S du virus de la mosaïque du choux fleur (CaMv35S) ou d'origine végétale tels que la petite sous unité du gène de la ribulose-l,5-bisphosphate carboxylase (RuBisCO) d'une culture comme par exemple le 3 plants derived from crosses using these plants transformed. It also aims at new promoters for the construction of the chimeric genes above.
More particularly, the subject of the invention is a chimeric gene to give plants a tolerance increased against a target herbicide EPSPS, including, in the sense of transcription, a promoter zone, a transit peptide zone, a sequence coding for a tolerance enzyme glyphosate and a polyadenylation signal zone, characterized in that the promoter zone is constituted at least one fragment of a promoter of a gene of vegetable histone allowing preferential expression herbicide tolerance protein in the areas accumulation of glyphosate.
In a preferred form, the invention comprises a transformed plant cell comprising a gene chimera comprising, in the sense of transcription, a promoter zone, a transit peptide zone, a sequence encoding a tolerance protein to a herbicide accumulating in growth tissues fast plant, and a signal zone of polyadenylation, characterized in that the area promoter comprises at least one promoter of a gene of vegetable histone allowing the expression of the protein tolerant to a herbicide in areas of accumulation of said herbicide in the plants, said herbicide tolerance of the transformed plants obtained at from said transformed plant cells being improved compared to plants not including said chimeric gene.
In another preferred form, the invention understand a process to improve the tolerance of Herbicide plants, comprising (i) transforming 3a plant cells with a chimeric gene comprising, in the meaning of transcription, a promoter zone, a transit peptide zone, a sequence encoding a tolerance protein to a herbicide accumulating in the rapidly growing tissues of plants, and a polyadenylation signal zone, characterized in that the promoter zone comprises at least minus a promoter of a plant histone gene allowing the expression of the tolerance protein vis-against a herbicide in areas of accumulation of herbicide in plants.
In another preferred form, the invention understand the use of a chimeric gene comprising, in the sense of transcription, a promoter zone, a transit peptide zone, a sequence encoding a tolerance protein to a herbicide accumulating in the rapidly growing tissues of plants, and a polyadenylation signal zone, for improve the tolerance of plants to herbicides, characterized in that the promoter zone comprises at least one promoter of a histone gene plant allowing the expression of the protein of tolerance to a herbicide in areas accumulation of said herbicide in plants.
The histone gene comes from a plant monodicotyledonous such as for example wheat, corn or rice or preferably a dicotyledonous plant such as for example alfalfa, sunflower, soya, rapeseed or preferably Arabidopsis thaliana. Cf Plant Mol .. Biol. Vol 8, 1987 p 179-191 Chaboute et al.
A histone gene of the type H3 or preferably H4, alone or in a form multiple, especially double.
The promoter zone of the chimeric gene according to the invention may furthermore advantageously comprise 3b less a fragment of a promoter of a gene expressing naturally in plants ie, for example a promoter of viral origin such as the promoter of 35S RNA from cauliflower mosaic virus (CaMv35S) or of vegetable origin such as the penny ribulose-1,5-bisphosphate gene unit carboxylase (RuBisCO) of a culture such as
4 maïs ou le tournesol.
La zone peptide de transit comprend,dans le sens de la transcription, au moins un peptide de transit d'un gène végétal codant pour une enzyme à
localisation plastidiale, une partie de séquence de la partie mature N terminale d'un gène végétal codant pour une enzyme à localisation plastidiale,puis un second peptide de transit d'un gène végétal codant pour une enzyme à localisation plastidiale,de préférence le gène de la RuBisCO
Les peptides de transit ci-dessus utilisables dans la zone de peptide de transit peuvent être en soi connus,d'origine végétale,par exemple issus de maïs, de tournesol, de pois, de tabac ou autres.Le premier et le second peptide de transit peuvent être identiques, analogues ou différents.Ils peuvent en outre comprendre chacun une ou plusieurs unités peptide de transit.
La partie de séquence de la partie mature N
terminale est issue d'un gène végétal codant pour une enzyme à localisation plastidiale, comme par exemple un gène de maïs,de tournesol,de pois ou autres,l'espèce végétale d'origine pouvant être identique,analogue ou différente de celle dont sont issus respectivement le premier et le second peptide de transit.Par ailleurs la partie de séquence de la partie mature peut comprendre un nombre variable d'acides aminés,généralement de 15 à
40,de préférence de 18 à 33.
La construction de l'ensemble de la zone de peptide de transit peut être de manière en soi connue,notamment par fusion ou tout autre moyen convenable.Cette zone caractéristique a comme rôle de permettre le relargage d'une protéine mature avecune efficacité maximale,de préférence sous forme native.
La séquence codante pour la tolérance 4 corn or sunflower.
The peptide transit zone comprises, in the sense of transcription, at least one peptide of transit of a plant gene encoding an enzyme to plastid localization, a sequence part of the N-terminal mature part of a plant gene coding for an enzyme with plastid localization, then a second transit peptide of a plant gene coding for a enzyme with plastid localization, preferably the gene RuBisCO
Transit peptides above usable in the transit peptide area can be per se known, of vegetable origin, for example from maize, sunflower, peas, tobacco or other.The first and the second transit peptide may be identical, analogous or different.They can furthermore understand each one or more transit peptide units.
The sequence part of the mature part N
terminal is derived from a plant gene coding for a plastid localization enzyme, such as for example a corn, sunflower, pea or other gene, the species plant of origin which may be identical, similar or different from that from which the first and second transit peptide.
sequence part of the mature part can understand a variable number of amino acids, generally from 15 to 40, preferably from 18 to 33.
The construction of the entire area of transit peptide can be in a way in itself known, in particular by fusion or any other means This characteristic zone has the role of allow the release of a mature protein with a maximum efficiency, preferably in native form.
The coding sequence for tolerance
5 herbicide utilisable dans le gène chirnère selon l'invention code pour une EPSPS mutée ayant un degré de tolérance au glyphosate. Cette séquence obtenue notamment par mutation du gène EPSPS peut être d'origine bactérienne, par exemple issu de Salmonella typhymurium (et nommée dans la suite "gène AroA"), ou végétale, par exemple de pétunia ou de tomate. Cette séquence peut comprendre une ou plusieurs mutations,par exemple la mutation Pro. 101 en Ser. ou encore les mutations Gly 96 en Ala.
La zone signal de polyadénylation,non traduite en 3' du géne chimère selon l'invention peut être d'origine quelconque,par exemple bactérienne telle que celle du gène de nopaline synthase,ou végétale telle que celle de la petite sous unité de la RuBisCO du maïs ou du tournesol.
Le gène chimère selon l'invention peut comprendre, en plus des parties essentielles ci-dessus, une zone intermédiaire non traduite(linker) entre la zone promotrice et la séquence codante et qui peut etre d'origine quelconque bactérienne,virale ou végétale.
EXEMPLE 1:CONSTRUCTI4N D'UN GENE CHIMERE :
On effectue la construction d'un gène chimère selon l'invention à partir des éléments:
1)Promoteur:on isole le promoteur à
partir dun clone respectivement d'histone H4 A777 et d'histone H4 A748 d'Arabidopsis thaliana race Strasbourg décrits par Chaboute(thèse de l'Université
de Strasbourg 1987 et PLant Mol. Biol. Vol 8, 1987 p 179-191). Ces promoteurs, comprenant environ lkpb entre les sites XhoI utilisés pour l'isoler,sont utilisés tels que ou sous forme dupliquée ou fusionnée avec un promoteur de CaMV35S seul ou double,c'est à 5 herbicide usable in the chirnene gene according to the invention encodes a mutated EPSPS having a degree of tolerance to glyphosate. This sequence obtained particularly by mutation of the EPSPS gene can be of bacterial origin, for example from Salmonella typhymurium (and hereinafter referred to as "AroA gene"), or vegetable, for example petunia or tomato. This sequence may include one or more mutations, by example the Pro mutation. 101 in Ser. or the Gly 96 mutations in Ala.
The polyadenylation signal zone, untranslated 3 'of the chimeric gene according to the invention can be of any origin, for example bacterial such as that of the nopaline synthase gene, or plant such that of the small sub-unit of RuBisCO maize or sunflower.
The chimeric gene according to the invention can understand, in addition to the essential parts above, an untranslated intermediate zone (linker) between promoter area and the coding sequence and that can be of any bacterial, viral or plant origin.
EXAMPLE 1: CONSTRUCTION OF A CHIMERIC GENE
The construction of a chimeric gene is carried out according to the invention from the elements:
1) Promoter: the promoter is isolated from a clone respectively of histone H4 A777 and of histone H4 A748 of Arabidopsis thaliana race Strasbourg described by Chaboute (University thesis of Strasbourg 1987 and PLant Mol. Biol. Vol 8, 1987 p 179-191). These promoters, including about lkpb between the XhoI sites used to isolate it, are used as or in duplicate or merged form with a single or double CaMV35S promoter, this is at
6 ~ï f) dire dont une partie a été dupliquée.
2)Zone de transfert:les deux peptides de transit ainsi que les éléments de protéines matures utilisés proviennent de l'ADNc cloné de la petite sous unité de la RuBisCO de maïs correspondant au gène décrit par Lebrun et al(1987) et de l'ADNc cloné de la petite sous unité de la RuBisCO de tournesol isolé par Waksman et al(1987).Plus précisément,la zone de transfert comprend,dans le sens de la traduction:
-un peptide de transit de la petite sous unité de la RuBisCO de tournesol, -une séquence de 22 acides aminés de la partie mature N terminale de de la petite sous unité de la RuBisCO de maïs, -un peptide de transit de la petite sous unité de la RuBisCO de maïs.
D'autres gènes analogues peuvent contenir respectivement des séquences de 10 à 40 et de préférence de 18 et 33 acides aminés.
Afin de fournir un élément comparatif,une autre construction a été effectuée contenant,dans le sens de la transcription "promoteur double CaMV35S/
peptide de transit de la PSU de la RuBisCO de tournesol/séquence N terminale de 22 acides aminés de la PSU de la RuBisCO de maïs/peptide de transit de la PSU de la RuBisCO de maïs/gène AroA/nos"(pRPA-BL 410).
3)Gène de structure:il provient du gène muté(Pro 101 en Ser) de l'EPSPS de Salmonella typhymurium isolé par Stalker et al(1985).Le clone pMG34-2(fourni par Calgene)a été linéarisé par XbaI
puis traité à la nucléase de Vigna radiata.Après recoupure par SmaI les deux extrémités franches ont été
ligaturées.Le clone obtenu possède un site NcoI sur l'ATG initiateur ainsi qu'un site SalI à 17pb en aval ~06183j 6 ~ ï f) say which part has been duplicated.
2) Transfer zone: the two peptides of transit as well as mature protein elements used come from the cloned cDNA of the little under RuBisCO unit of maize corresponding to the gene described by Lebrun et al (1987) and the cloned cDNA of small subunit of sunflower RuBisCO isolated by Waksman et al (1987). More precisely, the area of transfer includes, in the sense of translation:
a transit peptide of the small subunit of RuBisCO of sunflower, a sequence of 22 acids amines of the mature N-terminal part of the small sub-unit of RuBisCO of maize, a transit peptide of the small sub-unit of RuBisCO of maize.
Other similar genes may contain respectively sequences from 10 to 40 and preferably 18 and 33 amino acids.
In order to provide a comparative element, a another construction was carried out containing, in the transcriptional meaning "double CaMV35S promoter /
transit peptide of the RuBisCO PSU of sunflower / N-terminal sequence of 22 amino acids from the RuBisCO PSU of maize / transit peptide from the PSU RuBisCO corn / gene AroA / nos "(pRPA-BL 410).
3) Structural gene: it comes from the gene mutated (Pro 101 in Ser) from the Salmonella EPSPS
typhymurium isolated by Stalker et al (1985). The clone pMG34-2 (provided by Calgene) was linearized by XbaI
then treated with nuclease of Vigna radiata.After SmaI recut both ends were free The clone obtained has a NcoI site on the initiator ATG and a SalI site at 17pb downstream ~ 06183j
7 du codon stop.Ce clone a été nommé pRPA-BL 104.
4) Zone signal de polyadénylation:le fragment provient du gène de la nopaline synthase de pTi37 (Bevan et al,1983).Ce site est contenu dans un fragment MboI de 260pb(Fraley et al,1983;demande de brevet PCT 84/02913) qui a été traité par la polymérase de Klenow et cloné dans le site SmaI de M13 mp 18 pour introduire des sites BamHI et EcoRI respectivement aux extrémités 5' et 3'.
Après coupure par BamHI et traitement à la nucléase de Vigna radiata puis coupure EcoRI et traitement par la polymérase de Klenow,le fragment résultant a été introduit dans le vecteur p-BL 20(cf demande de brevet français 88/04130) coupé par XbaI et BamHI traités à la polymérase de Klenow. Après recoupure par SalI et SstI,on obtient un fragment d'environ 0,4kpb contenant la séquence nos 3' du côté
du site Sal I et la bordure droite de l'ADN-T du côté
du site SstI.
L'assemblage de tous ces éléments a été
effectué de la façon suivante:
Fusion" peptide de transit de la PSU de la RuBisCO
de maïs/gène AroA":
Le peptide de transit de la PSU du gène de la RuBisCO de maïs provient d'uri fragment EcoRI-SphI de 192pb issu de l'ADNc correspondant au gène de la PSU du gène de la RuBisCO de maïs,décrit par Lebrun et al(1987),possédant un site NcoI recouvrant le codon initiateur de la traduction et un site SphI
correspondant au site de clivage du peptide de transit.
Par traitement de l'extrémité SphI avec la polymérase du bactériophage T4 et en la ligaturant avec l'extrémité NcoI,traitée à la polymérase de Klenow,du gène AroA de pRPA-BL 104 recoupé EcoRI,on obtient la , _ ~
r,~ i >>~:~~ 7 of the stop codon. This clone was named pRPA-BL 104.
4) Polyadenylation signal area: the fragment comes from the nopaline synthase gene of pTi37 (Bevan et al, 1983). This site is contained in a MboI fragment of 260bp (Fraley et al, 1983;
PCT Patent 84/02913) which has been treated with the polymerase from Klenow and cloned into the SmaI site of M13 mp 18 for introduce BamHI and EcoRI sites respectively into 5 'and 3' ends.
After cleavage with BamHI and treatment with nuclease of Vigna radiata then cut EcoRI and Klenow polymerase treatment, the fragment resultant was introduced into the vector p-BL 20 (cf.
French patent application 88/04130) cut by XbaI and BamHI treated with Klenow polymerase. After recut with SalI and SstI, we get a fragment about 0.4kbp containing the sequence nos 3 'on the side of the Sal I site and the right border of the T-DNA from the of the SstI website.
The assembly of all these elements has been performed as follows:
Fusion "peptide transit of the RuBisCO PSU
of corn / AroA gene ":
The transit peptide of the PSU of the gene of the RuBisCO of maize originates from an EcoRI-SphI fragment of 192bp from the cDNA corresponding to the gene of the PSU of the RuBisCO gene of corn, described by Lebrun and al (1987), having a NcoI site covering the codon initiator of the translation and a site SphI
corresponding to the cleavage site of the transit peptide.
By treating the SphI end with the bacteriophage T4 polymerase and ligate it with the NcoI end, treated with Klenow polymerase, AroA gene of pRPA-BL 104 cut EcoRI, we obtain the , _ ~
r, ~ i >> ~: ~~
8 fusion traductionelle entre le peptide de transit de maïs et le gène de l'EPSPS bactérienne.
Fusion peptide de transitde la PSU de la RuBisCO
de maïs/séquence de 22 acides aminés de ]a par_tie mature du gène de maïs/ gène AroA:
De façon similaire un fragment EcoRi-Hindil de 228bp de l'ADNc de la PSU du gène de la RuBisCO de maïs est ligaturé avec l'extrémité NcoI traitée à la polymérase de Klenow du gène AroA de pRPA-BL 104 et recoupé par EcoRI. On obtient une fusion traductionnelle entre le peptide de transit de la PSU
de la RuBisCO de maïs,les 22 acides aminés de la partie mature de la PSU de la RuBisCO de maïs et le gène de l'EPSPS bactérienne.
Peptide de transit de la PSU de la RuBisCO de tournesol:
Le fragment est issu de l'ADNc isolé par Waksman et Freyssinet(1987). Un site SphI a été créé
selon la méthode de Zoller et Smith (1984) au site de clivage du peptide de transit.Le peptide de transit de la PSU de la RuBisCO de tournesol ainsi obtenu est un fragment EcoRI-SphI de 171 pb.
Fusion peptide de transit de la PSU de la RuBisCO
de tournesol/séquence de 22 acides aminés de la partie mature de la PSU de la RuBisCO de maïs/ gène AroA:
La construction contenant la fusion peptide de transit de la PSU de la RuBisCO de maïs/séquence de 22 acides aminés de la PSU de la RuBisCO de maïs a été
coupée par EcoRI-SphI puis mis en ligation avec le fragment EcoRI-SphI de 171 pb correspondant au peptide de transit de la PSU de la RuBisCO de tournesol. Une construction résultante présente une substitution des fragments EcoRI-SphI et est une fusion traductionnelle "peptide de transit de la PSU de la RuBisCO de ~à ,~.~ 8,3)~ 8 translational fusion between the transit peptide of corn and the bacterial EPSPS gene.
Transit peptide fusion of the RuBisCO PSU
of corn / 22 amino acid sequence of mature corn gene / AroA gene:
Similarly, an EcoRi-Hindil fragment of 228bp cDNA of the PSU of RuBisCO gene of corn is ligated with the NcoI end treated at the Klenow polymerase of the AroA gene of pRPA-BL 104 and intersected by EcoRI. We obtain a fusion translation between transit peptide of the PSU
RuBisCO of corn, the 22 amino acids of the game mature of the RuBisCO PSU of corn and the gene of bacterial EPSPS.
Transit peptide of the RuBisCO PSU of sunflower:
The fragment is derived from cDNA isolated by Waksman and Freyssinet (1987). An SphI site has been created according to the method of Zoller and Smith (1984) at the site of cleavage of the transit peptide.The transit peptide of the RuBisCO PSU of sunflower thus obtained is a EcoRI-SphI fragment of 171 bp.
Transit peptide fusion of the RuBisCO PSU
of sunflower / sequence of 22 amino acids of the party mature of the RuBisCO PSU of maize / AroA gene:
The construction containing the peptide fusion of transit of the maize RuBisCO PSU / sequence of 22 Amino acids of the RuBisCO PSU of maize has been cut by EcoRI-SphI and then ligation with the EcoRI-SphI fragment of 171 bp corresponding to the peptide transit of the RuBisCO PSU of sunflower. A
resulting construction shows a substitution of EcoRI-SphI fragments and is a translational fusion "transit peptide of the RuBisCO PSU of ~ to, ~. ~ 8,3) ~
9 tournesol/séquence de 22 acides aminés de la PSU de la RuBisCO de maïs/gène AroA.
Le fragment EcoRi-Sa.lI a été ligaturé avec le fragment SalI-SstI contenantla séquence nos 3' et la bordure droite de l'ADN-T. Le fragment EcoRI-SstI
résultant comprenant"peptide de transit de la PSU de la RuBisCO de tournesol/séquence de 22 acides aminés de la PSU de la RuBisCO de maïs/gène AroA/nos 3'/Bordure droite ADN-T" est substitué au fragment EcoRI-SstI
contenant la bordure droite de l'ADN-T du plasmide 150 A alpha 2 contenant le promoteur double CaMV. La fusion transcriptionelle "double CaMV/peptide de transit de la PSU de la RuBisCO de tournesol/séquence de 22 acides aminés de la PSU de la RuBisCO de maïs/gène AroA/nos 3' dans le vecteur 150 A alpha 2 a été nommé pRPA-BL 294.
Fusion"peptide de transit de la PSU de la RuBisCO
de tournesol/séguence de 22 acides aminés de la PSU de la RuBisCO de maïs/peptide de transit de la PSU de la RuBisCO de maïs/gène AroA":
La construction ci-dessus est coupée par NcoI-HindiiI libérant le gène AroA.Puis elle est mise en ligation avec un fragment NcoI-Hind III de 1,5kpb contenant la fusion"peptide de transit de la PSU de la RuBisCO de maïs/gène AroA".Une construction résultante présente une substitution des fragments NcoI-HindIII et est une fusion traductionelle "peptide de transit de la PSU de la RuBisCO de tournesol/séquence de 22 acides aminés de la PSU de la RuBisCO de maïs/peptide de transit de la PSU de la RuBisCO de maïs/gène AroA".
Le fragment EcoRI-SalI a été ligaturé avec le fragment SalI-SstI contenantla séquence nos 3' et la bordure droite de l'ADN-T.Le fragment EcoRI-SstI
résultant comprenant"peptide de transit de la PSU de la RuBisCO de tournesol/séquence de 22 acides aminés de la ti.1 PSU de la RuBisCO de maïs/peptide de transit de la PSU
de RuBisCO de maïs/gène AroA/nos 3'/Bordure droite ADN-T" est substitué au fragment EcoRI-SstI contenant la bordure droite de l'ADN-T du plasmide 150 A alpha 2 5 contenant le promoteur double CaMV. La fusion transcriptionelle "double CaMV/peptide de transit de la PSU de la RuBisCO de tournesol/séquence de 22 acides aminésde la PSU de la RuBisCO de niaïs/peptide de transit de la PSU de la RuBisCO de maïs/gène AroA/nos 9 sunflower / sequence of 22 amino acids from the PSU of the RuBisCO of corn / AroA gene.
The EcoRiSaII fragment was ligated with the SalI-SstI fragment containing the sequence nos 3 'and the right border of the T-DNA. The EcoRI-SstI fragment resultant comprising "transit peptide of the PSU of the RuBisCO of Sunflower / Sequence of 22 amino acids from the PSU of RuBisCO of maize / AroA gene / nos 3 '/ Border straight T-DNA is substituted for the EcoRI-SstI fragment containing the right border of the T-DNA of plasmid 150 A alpha 2 containing the CaMV double promoter. Fusion transcriptional "double CaMV / transit peptide of the Sunflower RuBisCO PSU / Sequence of 22 Acids amines of the RuBisCO PSU of maize / AroA gene / nos 3 ' in the 150A alpha 2 vector was named pRPA-BL 294.
Fusion "peptide transit of the RuBisCO PSU
of sunflower / segregation of 22 amino acids from the PSU of RuBisCO of maize / transit peptide from the PSU of the RuBisCO of maize / AroA gene ":
The above construction is cut by NcoI-HindIII releasing the AroA gene.Then it is implemented ligation with a 1.5 kbp NcoI-Hind III fragment containing the fusion peptide transit of the PSU of the RuBisCO of corn / AroA gene ".A resultant construct shows a substitution of the NcoI-HindIII fragments and is a translational fusion "transit peptide of the Sunflower RuBisCO PSU / Sequence of 22 Acids amines of the RuBisCO PSU of maize / peptide transit of the RuBisCO PSU of maize / AroA gene ".
The EcoRI-SalI fragment was ligated with the SalI-SstI fragment containing the sequence nos 3 'and the right border of the T-DNA. The EcoRI-SstI fragment resultant comprising "transit peptide of the PSU of the RuBisCO of Sunflower / Sequence of 22 amino acids from the ti.1 PSU of RuBisCO maize / peptide transit PSU
of corn RuBisCO / AroA gene / nos 3 '/ Right border DNA-T "is substituted for the EcoRI-SstI fragment containing the right border of the T-DNA of plasmid 150 A alpha 2 5 containing the CaMV double promoter. Fusion transcriptional "double CaMV / transit peptide of the Sunflower RuBisCO PSU / Sequence of 22 Acids Amines of the RuBisCO PSU of Niais / Peptide transit of the RuBisCO PSU of maize / AroA gene / nos
10 3' dans le vecteur 150 A alpha 2 a été nommé pRPA-BL
410.
Toutes les constructions ont été obtenues par substitution de la zone promotrice double CaMV de la construction pRPA-BL 410 obtenue ci dessus,coupée en EcoRi-HindliI par un fragment HindiII-EcoRi contenant les différents éléments de promoteurs suivants:
A)Promoteur d'histone simple H4 A748 Un fragment XhoI-XhoI d'environ 1 kpb contenant le promoteur d'histone H4 748 d'Arabidopsis thaliana cf PLant Mol.Biol. Vol. 8, 1987 p 179-191 a été ligaturé
avec pUC 19 coupé par SalI. Ce clone a ensuite été
coupé par XbaI traité à la polymérase de Klénow et EcoRI traité à la polymérase de Klénow puis ligaturé en condition favorisant la recircularisation.Le fragment HindiIi-EcoRi contenant le promoteur histone a été
substitué au fragment Hind III-EcoRi contenant le promoteur double CaMV de pRPA-BL 410.
Le clone résultant contient"promoteur d'histone H4/peptide de transit de la PSU de la RuBisCO de tournesol/séquence de 22 acides aminés de la PSU de la RuBisCO de maïs/peptide de transit de la PSU de la RuBisCO de maïs/gène AroA/nos" et a été nommé pRPA-BL
498.
B)Promoteur d'histone simple H4 777 ~t CJ ca ~ 3 'in the vector 150A alpha 2 was named pRPA-BL
410.
All constructions were obtained by substitution of the double CaMV promoter zone of the pRPA-BL 410 construction obtained above, cut in EcoRI-HindIII with a HindIII-EcoRI fragment containing the following elements of promoters:
A) Simple histone promoter H4 A748 An XhoI-XhoI fragment of about 1 kbp containing the histone promoter H4 748 of Arabidopsis thaliana cf PLant Mol.Biol. Flight. 8, 1987 p 179-191 was ligated with pUC 19 cut by SalI. This clone was then cut with Klenow polymerase-treated XbaI and EcoRI treated with Klenow polymerase and then ligated into condition favoring recircularisation.The fragment HindIII-EcoRI containing the histone promoter was substituted for the Hind III-EcoRi fragment containing the CaMV double promoter of pRPA-BL 410.
The resulting clone contains "histone promoter H4 / transit peptide of the RuBisCO PSU of sunflower / sequence of 22 amino acids from the PSU of the RuBisCO of maize / transit peptide from the PSU of the RuBisCO of maize / AroA gene / nos "and was named pRPA-BL
498.
B) Single Histone Promoter H4 777 ~ t CJ ca ~
11 Un fragment Xhol de 1 kpb environ contenant l'ensemble des régions 5' proximale du gène d'histone H4 777 d'Arabidopsis thaliana cf Plant Mol.Biol. Vol.8, 1987 p 179-191 a été cloné au site Sal I du plasmide pUC 19 dans une orientation telle que les sites du polylinker de pUC 19 de XbaI à EcoRI soit situés en aval du site d'initiation de la transcription.
Fusion zone de transit de PSU de RuBisCO de tournesol/AroA
Un fragment EcoRI - Hinc II de l'ADNc de la PSU de RuBisCO de tournesol isolé par Waksman et Freyssinet (1987) codant pour le peptide de transit et 30 acides aminés de la proteine mature a été cloné aux sites EcoRI et Sma I de pUC 18.
Un fragment EcoRI-XbaI a été isolé et inséré en amont du gène AroA de pMG 34-2 (fourni par Calgene) aux sites EcoRI et XbaI. Afin de mettre en phase les 2 régions codantes, l'insert EcoRI-Hind III de ce clone a été inséré dans M13 mp19 aux sites EcoRI et Hind III.
La forme réplicative de l'ADN de ce clone a été
linéarisé par XbaI puis traité par la nuclease de Vigna radiata. Après ligation dans des conditions favorisant la recircularisation et transformation, l'ADN de certains clones a été analysé par sequençage. Un des clones obtenu réalise une fusion traductionnelle entre l'élément de PSU de RuBisCO et le fragment AroA, le codon initiateur ATG de ce dernier étant perdu. La séquence de la jonction entre ces deux éléments est la suivante GAC GGGGATCCGGAA
PSU Linker AroA.
Cette fusion comporte donc dans le sens de la 4'u DI û 11 An XhoI fragment of about 1 kbp containing the set of 5 'proximal regions of the histone gene H4 777 from Arabidopsis thaliana cf Plant Mol.Biol. Vol.8, 1987 p 179-191 was cloned at the Sal I site of the plasmid pUC 19 in an orientation such as the sites of the polylinker from pUC 19 from XbaI to EcoRI are located in downstream of the transcription initiation site.
Fusion RuBisCO PSU transit area of sunflower / AroA
An EcoRI-Hinc II fragment of the PSU cDNA
RuBisCO sunflower isolated by Waksman and Freyssinet (1987) coding for the transit peptide and 30 acids amines of the mature protein has been cloned at sites EcoRI and Sma I from pUC 18.
An EcoRI-XbaI fragment was isolated and inserted into upstream of the pMG 34-2 AroA gene (provided by Calgene) to EcoRI and XbaI sites. In order to match the 2 coding regions, the EcoRI-Hind III insert of this clone has was inserted into M13 mp19 at the EcoRI and Hind III sites.
The replicative form of the DNA of this clone has been linearized by XbaI then treated with Vigna nuclease radiata. After ligation in favorable conditions recircularization and transformation, the DNA of some clones were analyzed by sequencing. One of clones got performs a translational fusion between the PSU element of RuBisCO and the AroA fragment, the ATG initiator codon of the latter being lost. The sequence of the junction between these two elements is the next GAC GGGGATCCGGAA
PSU Linker AroA.
This merger therefore includes, in the sense of 4 'DI
12 traduction : peptide de transit de la PSU de RuBisCO de tournesol/30 acides aminés de la partie mature de la PSU de RuBisCO de tournesol/3 acides aminés correspondant au linker intermédiaire/AroA.
Construction de pRPA - BL - 240 Le plasmide comprenant le promoteur du gène histone H4 777 décrit ci-dessus a été coupé par XbaI, traité par la polymerase de Klenow et le fragment résultant de la recoupure par Hind III, isolé. Le plasmide contenant la fusion peptide de transit de tournesol/AroA décrite ci-dessus a été coupé par EcoRI, traité par la polymérase de Klenow et le fragment résultant de la recoupure par Hind III isolé. Ces deux fragments ont été mis en ligation en présence de pUC 19 coupé par Hind III. Un des clones résultant présente la structure suivante : promoteur his-tone/zone codant pour le peptide de transit de la PSU de RuBisCO de tournesol/zone codant pour 30 acides aminés de la partie mature de la PSU de la RuBisCO de tournesol/zone codant pour 3 acides aminés correspondant au linker intermédiaire/zone codant pour AroA.
Ce clone a été coupé par Sal I, traité par la polymérase de Klenow, puis après recoupure par Hind III
le fragment isolé a été ligaturé avec le plasmide contenant la zone de polyadénylation coupé par Bam HI, traité par la polymérase de Klenow, puis recoupé par Hind III.
Un des clones résultant présente la structure suivante : promoteur histone/zone codant pour le peptide de transit de la PSU de RuBisCO de tournesol/zone codant pour 30 acides aminés de la partie mature de RuBisCO de tournesol/zone codant pour 3 acides aminés correspondant au linker intermédiaire/zone codant pour AroA/nos3'. 12 translation: transit peptide of the RuBisCO PSU of sunflower / 30 amino acids from the mature part of the Sunflower RuBisCO PSU / 3 Amino Acids corresponding to the intermediate linker / AroA.
Construction of pRPA - BL - 240 The plasmid comprising the gene promoter histone H4 777 described above was cut by XbaI, treated with Klenow polymerase and the fragment resulting from Hind III cutback, isolated. The plasmid containing the transit peptide fusion of sunflower / AroA described above was cut by EcoRI, treated with Klenow polymerase and the fragment resulting from the isolated Hind III recut. These two fragments were ligated in the presence of pUC 19 cut by Hind III. One of the resulting clones presents the following structure: his-tone promoter / coding zone for the transit peptide of the RuBisCO PSU of sunflower / zone coding for 30 amino acids of the Mature part of the RuBisCO PSU of Sunflower / Area coding for 3 amino acids corresponding to the linker intermediate / coding zone for AroA.
This clone was cut by Sal I, treated by the Klenow polymerase, then after Hind III recut the isolated fragment was ligated with the plasmid containing the Bam HI cut polyadenylation zone, treated with Klenow polymerase, then cross-checked by Hind III.
One of the resulting clones has the structure following: histone promoter / zone coding for the transit peptide of the RuBisCO PSU of sunflower / zone coding for 30 amino acids of the RuBisCO mature part of sunflower / coding area for 3 amino acids corresponding to the linker intermediate / coding zone for AroA / nos3 '.
13 Le plasmide ci-dessus a été linéarisé par Hind IIT
et inséré au site unique Hind III du irecteur pRPA-BL
127 construit de la façon suivante : le vecteur pCGN
1152 possèdant un gène de résistance à l'hygromycine sous contrôle du gène de la mannopine synthase et du terminateur du gène Tml (fourni par Calgene) a été
digéré par Hind III et religaturé sur lui même, conduisant à la création d'un site unique de clonage Hind III.
Un des clones résultant comporte la fusion transcriptionnelle suivante en partant de la bordure gauche de l'ADN-T du plasmide pRPA-BL 127 : promoteur histone/zone de transit de PSU de RuBisCO de tournesol/AroA/nos3' et a été nommé pRPA-BL-240.
C) Duplication du promoteur d'histone (= promoteur double histone).
Le promoteur histone H4 dans pUC 19 décrit ci-dessus a été dirigé par NdeI, traité par la polymérase de Klénow, puis recoupé par Hind III. Le fragment éliminé a été substitué par un fragment Hind III -EcoRV purifié par digestion du plasmide portant le promoteur histone H4. Un des clones obtenu a la structure suivante : zone 5' du promoteur H4 de Hind III à Nde I de 530 pb, zone dupliquée correspondant à
deux fragments de 330 pb de NdeI à EcoRV directement répétés, zone 3' du promoteur H4 de EcoRV à EcoRI de 140 pb.
Le fragment Hind IIi-EcoRi contenant le promoteur double histone a été substitué au fragment Hind III-EcoRi contenant le double CaMV de pRPA-BL 410. Le clone résultant contient"double promoteur histone/peptide de transit de la PSU de la RuBisCO de tournesol/séquence de 22 acides aminés de la PSU de la RuBisCO de maïs/peptide de transit de maïs/gène AroA/nos" et a été
J 13 The plasmid above was linearized by Hind IIT
and inserted at the unique Hind III site of the pRPA-BL irector 127 constructed in the following way: the vector pCGN
1152 with a hygromycin resistance gene under the control of the gene for mannopine synthase and terminator of the Tml gene (provided by Calgene) was digested with Hind III and religated on itself, leading to the creation of a unique cloning site Hind III.
One of the resulting clones involves fusion next transcriptional starting from the border left of the T-DNA of the plasmid pRPA-BL 127: promoter histone / RuBisCO PSU transit area of sunflower / AroA / nos3 'and was named pRPA-BL-240.
C) Duplication of the histone promoter (= promoter double histone).
The histone promoter H4 in pUC 19 described above top was directed by NdeI, treated with polymerase of Klénow, then intersected by Hind III. The Shard removed was substituted with a Hind III fragment -EcoRV purified by digestion of the plasmid carrying the histone promoter H4. One of the clones obtained at the following structure: 5 'zone of Hind H4 promoter III to Nde I of 530 bp, duplicated area corresponding to two 330 bp fragments of NdeI to EcoRV directly 3 'region of the EcoRV to EcoRI H4 promoter from 140 bp.
The Hind III-EcoRI fragment containing the promoter double histone was substituted for the Hind III fragment EcoRi containing the double CaMV of pRPA-BL 410. The clone resulting contains "double histone promoter / peptide transit of the sunflower RuBisCO PSU / sequence of 22 amino acids from the PSU of RuBisCO's corn / maize transit peptide / AroA gene / nos "and has been J
14 nommé pRPA-BL 488.
D)Promoteur hybride double CaMV/histone:
Le promoteur histone H4 A748,dans la cassette HindiIi-EcoRi décrite ci-dessus(promoteur histone simple H4 A748),est coupé AccI,traité à la polymérase de Klenow puis coupé EcoRI.Le fragment résultant de 580pb est ligaturé avec le promoteur double CaMV coupé
EcoRV-EcoRI.Le clone résultant comprenant la fusion double CaMV partie 3' du promoteur histone est coupé
HindlIi-EcoRi et substitué au fragment Hindili-EcoRi de pRPA-BL 410 comprenant le double CaMV. La construction résultante comprend"promoteur double CaMV/partie 31 promoteur histone/peptide de transit de la PSU de la RuBisCO de tournesol/séquence de 22 acides aminés de la PSU de la RuBisCO de maïs/peptide de transit de la PSU
de la RuBisCO de maïs/gène AroA/nos" et a été nommé
pRPA-BL 502.
EXEMPLE 2:RESISTANCE DES PLANTES TRANSFORMEES
1 Transformation:
Le vecteur est introduit dans la souche non oncogène d'Agrobacterium EHA 101(Hood et al,1987)porteuse du cosmide pTVK 291(Komari et al,1986).La technique de transformation est basée sur la procédure de Horsh et al(1985).
2 Régénération:
La régénération du tabac PBD6(provenance SEITA France) à partir d'explants foliaires est réalisée sur un milieu de base Murashige et Skoog(MS) comprenant 30g/1 de saccharose ainsi que 200ug/ml de kanamycine.Les explants foliaires sont prélevés sur des plants en serre ou in vitro et transformés selon la technique des disques foliaires(Science 1985,Vol 227,p.1229-1231) en trois étapes successives:la première comprend l'induction des pousses sur un milieu MS additionné de 30g de saccharose contenant 0.05mg d'acide naphtylacétique (ANA) et 2 mg/1 de benzylaminopurine (BAP) pendant 15 jours.Les pousses 5 formées au cours de cette étape sont ensuite développées par culture sur un milieu MS additionné de 30 g/l de saccharose mais ne contenant pas d'hormone,pendant 10 jours.Puis on prélève des pousses développées et on les cul-tive sur un milieu 10 d'enracinement MS dilué au demi à teneur moitié en sels, vitamines et sucres et ne contenant pas d'hormone.Au bout d'environ 15 jours,les pousses enracinées sont passées en terre. Des plants de tabac PBD6 non transformés ont été pris au même stade à titre 14 named pRPA-BL 488.
D) CaMV / histone double hybrid promoter:
The histone promoter H4 A748, in the cassette HindIII-EcoRI described above (histone promoter single H4 A748), is cut AccI, polymerase-treated Klenow then cut EcoRI.The fragment resulting from 580pb is ligated with the CaMV double cut promoter EcoRV-EcoRI.The resulting clone comprising fusion double CaMV part 3 'of the histone promoter is cut HindIII-EcoRi and substituted for the HindIII-EcoRi fragment of pRPA-BL 410 comprising double CaMV. Construction resultant comprises CaMV double promoter / part 31 histone / peptide transit promoter of the PSU of the RuBisCO of Sunflower / Sequence of 22 amino acids from the PSU of RuBisCO maize / peptide transit PSU
of RuBisCO of corn / AroA gene / nos "and was named pRPA-BL 502.
EXAMPLE 2: RESISTANCE OF TRANSFORMED PLANTS
1 Transformation:
The vector is introduced into the strain non-oncogene of Agrobacterium EHA 101 (Hood and al, 1987) carrier of cosmid pTVK 291 (Komari and al, 1986) .The transformation technique is based on the procedure of Horsh et al (1985).
2 Regeneration:
Regeneration of tobacco PBD6 (provenance SEITA France) from foliar explants is performed on a Murashige and Skoog (MS) core medium comprising 30 g / l of sucrose and 200 μg / ml of kanamycin.Foliary explants are taken from greenhouse or in vitro plants and processed according to technique of leaf discs (Science 1985, Vol.
227, p.1229-1231) in three successive stages: the first includes the induction of shoots on a medium MS supplemented with 30g of sucrose containing 0.05mg of naphthylacetic acid (ANA) and 2 mg / l of benzylaminopurine (BAP) for 15 days.
5 formed during this stage are then developed by culture on an MS medium supplemented with 30 g / l of sucrose but not containing of hormone, for 10 days.Then we take shoots developed and they are grown on a medium 10% of rooting DM diluted half to half content salts, vitamins and sugars and not containing After about 15 days, the shoots rooted have passed into the ground. Tobacco plants Unprocessed PBD6 were taken at the same stage as
15 de témoins.
3'Mesure de la tolérance au glyphosate:
les meilleurs plantes issues de la régénération des tabacs transformés sont sélectionnées en serre après traitement des plantes,au stade 5 feuilles par pulvérisation avec une suspension aqueuse de glyphosate à une dose correspondant à 0,6kg/ha de matière active.Les plantes sélectionnées ont été
autofécondées et les graines semées sur milieu MS
additionné de 30g/1 de sucrose et 200microg/ml de kanamycine.Les graines issues de plantes présentant un ratio de ségrégation de 3/4 de plantes résistantes-1/4 de plantes sensibles ont été conservées Une analyse par hybridation moléculaire a permis de déterminer les plantes n'ayant intégré qu'une copie de l'ADN-T.Par croisement et sélection,ces plantes ont été amenées à
l'état hétérozygotes ou homozygotes.Ces plantes ont été
semées en conditions naturelles de plein champ et pulvérisées au stade 5 feuilles avec une dose de *
0,8kg/ha de glyphosate (Round Up).Les résultats *m.c. 15 witnesses.
3'Measure of glyphosate tolerance:
the best plants from the regeneration of processed tobaccos are selected in the greenhouse after plant treatment, at stage 5 leaves by spraying with an aqueous suspension glyphosate at a dose corresponding to 0.6 kg / ha of active ingredient.The selected plants have been self-fertilized and seeds sown on MS medium supplemented with 30g / l of sucrose and 200microg / ml of kanamycin.Seeds from plants with a segregation ratio of 3/4 of resistant plants-1/4 of susceptible plants have been preserved An analysis molecular hybridization has made it possible to determine plants with only one copy of DNA-T.Par crossing and selection, these plants were brought to state heterozygotes or homozygotes.These plants have been sown in natural field conditions and sprayed at the 5-leaf stage with a dose of *
0.8kg / ha glyphosate (Round Up) .The results * mc
16 correspondants à l'observation d'indices de phytotoxicité relevés au bout de 30 jours après le traitement. Dans ces conditions on constate qu, les plants transformés par les constructions présentent iane tolérance acceptable (pRPA-BL 240 et 410) voire bonne (pRPA-BL 488 et 502) alors que les plants témoins sont complètement détruits;
Ces résultats montrent clairement l'amélioration apportéé par utilisation d'un gène chimère selon l'invention pour un même gène codant pour la tolérance au glyphosate.
Les plantes transformées selon l'invention peuvent être utilisées comme parents pour l'obtention de lignées et d'hybrides ayant une tolérance accrue au glyphosate.
Exemple 3 Des colzas de printemps, cultivar Westar, résistant au glyphosate, ont été obtenus en utilisant la technique de BOULTER et al., 1990 (Plant Science, 70: 91-99) avec les constructions pRPA-BL 488 (dH-At-PTO-aroA-nos), pRPA-BL 502 (CaMV/H--At-PT -aroA-nos).
Ces plantes ont résisté à un traitement en serre au glyphosate à 400 g m.a./ha, traitement qui détruit les plantes non transgéniques. 16 corresponding to the observation of indices of phytotoxicity recorded after 30 days after treatment. In these circumstances, it can be seen that plants transformed by the constructions present iane acceptable tolerance (pRPA-BL 240 and 410) or good (pRPA-BL 488 and 502) while the control plants are completely destroyed;
These results clearly show the improvement brought about by the use of a gene chimera according to the invention for the same gene coding for tolerance to glyphosate.
Transformed plants according to the invention can be used as parents to obtain lines and hybrids with increased tolerance to glyphosate.
Example 3 Spring colzas, Westar cultivar, glyphosate resistant, were obtained using the technique of BOULTER et al., 1990 (Plant Science, 70: 91-99) with the constructs pRPA-BL 488 (dH-At-PTO-aroA-nos), pRPA-BL 502 (CaMV / H - At-PT -aroA-nos).
These plants resisted greenhouse treatment at glyphosate at 400 g ai / ha, a treatment that destroys non-transgenic plants.
Claims (17)
localisation plastidiale, une partie de séquence de la partie mature N-terminale d'un gène végétal codant pour une enzyme à
localisation plastidiale, puis un second peptide de transit d'un gène végétal codant pour une enzyme à localisation plastidiale. 15- Plant cell transformed according to one of the Claims 1 to 14, characterized in that the peptide zone of transit is a sequence encoding a transit peptide comprising, in the direction of transcription, at least one peptide of transit of a plant gene coding for an enzyme to plastid localization, part of sequence of the part mature N-terminus of a plant gene encoding an enzyme to plastid localization, then a second transit peptide of a plant gene encoding an enzyme with plastid localization.
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Family Cites Families (5)
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US4940835A (en) * | 1985-10-29 | 1990-07-10 | Monsanto Company | Glyphosate-resistant plants |
US4971908A (en) * | 1987-05-26 | 1990-11-20 | Monsanto Company | Glyphosate-tolerant 5-enolpyruvyl-3-phosphoshikimate synthase |
US4875166A (en) * | 1987-10-09 | 1989-10-17 | Input/Output, Inc. | Bandwidth enhancing seismic acquisition system and method |
WO1990002172A1 (en) * | 1988-08-18 | 1990-03-08 | Calgene, Inc. | Plant elongation factor, promoters, coding sequences and uses |
FR2673642B1 (en) * | 1991-03-05 | 1994-08-12 | Rhone Poulenc Agrochimie | CHIMERIC GENE COMPRISING A PROMOTER CAPABLE OF GIVING INCREASED TOLERANCE TO GLYPHOSATE. |
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1991
- 1991-03-05 FR FR919102873A patent/FR2673642B1/en not_active Expired - Lifetime
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1992
- 1992-02-25 CA CA002061835A patent/CA2061835C/en not_active Expired - Lifetime
- 1992-02-26 BR BR929200789A patent/BR9200789A/en not_active IP Right Cessation
- 1992-03-02 IL IL101116A patent/IL101116A/en not_active IP Right Cessation
- 1992-03-03 MX MX9200916A patent/MX9200916A/en unknown
- 1992-03-04 IE IE069292A patent/IE920692A1/en not_active IP Right Cessation
- 1992-03-04 AT AT92420065T patent/ATE409233T1/en not_active IP Right Cessation
- 1992-03-04 ES ES92420065T patent/ES2309984T3/en not_active Expired - Lifetime
- 1992-03-04 PH PH44003A patent/PH31176A/en unknown
- 1992-03-04 AU AU11443/92A patent/AU652417B2/en not_active Expired
- 1992-03-04 DE DE69233747T patent/DE69233747D1/en not_active Expired - Lifetime
- 1992-03-04 EP EP92420065A patent/EP0507698B1/en not_active Expired - Lifetime
- 1992-03-05 KR KR1019920003658A patent/KR100259991B1/en not_active IP Right Cessation
- 1992-03-05 ZA ZA921646A patent/ZA921646B/en unknown
- 1992-03-05 JP JP04889492A patent/JP4303322B2/en not_active Expired - Lifetime
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1994
- 1994-05-09 US US08/239,947 patent/US5491288A/en not_active Expired - Lifetime
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AU652417B2 (en) | 1994-08-25 |
FR2673642B1 (en) | 1994-08-12 |
ATE409233T1 (en) | 2008-10-15 |
ZA921646B (en) | 1992-11-25 |
ES2309984T3 (en) | 2008-12-16 |
US5491288A (en) | 1996-02-13 |
CA2061835A1 (en) | 1992-09-06 |
KR100259991B1 (en) | 2000-06-15 |
MX9200916A (en) | 1992-09-01 |
PH31176A (en) | 1998-03-20 |
IL101116A (en) | 2007-07-04 |
BR9200789A (en) | 1992-11-17 |
DE69233747D1 (en) | 2008-11-06 |
IL101116A0 (en) | 1992-11-15 |
EP0507698A1 (en) | 1992-10-07 |
FR2673642A1 (en) | 1992-09-11 |
JPH0576369A (en) | 1993-03-30 |
US5792930A (en) | 1998-08-11 |
EP0507698B1 (en) | 2008-09-24 |
KR920018221A (en) | 1992-10-21 |
JP4303322B2 (en) | 2009-07-29 |
AU1144392A (en) | 1992-09-10 |
IE920692A1 (en) | 1992-09-09 |
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